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Securities Code•4559
Business ReportFrom April 1st, 2015 to March 31st, 2016
ContentsTo Our Shareholders …………………………………………… P.1Summary of Our Business Operations (Consolidated) ……… P.3Status of Research and Development ………………………… P.5Research and Development Pipeline ………………………… P.6Status of Production and Distribution / Outlook for Fiscal Year 2016 ………………………………… P.7Special Offers to Our Shareholders …………………………… P.8Topics …………………………………………………………… P.9Financial Statements (Consolidated) ……………………… P.11Company Information ……………………………………… P.13Share Information …………………………………………… P.14Shareholder Memo
62nd
President and COO
Mitsuhiro Ibe
We, Zeria Pharmaceutical Co., Ltd. (“Zeria”) would like to express our thanks for your particular support, and we would like to express our deepest condolences and sympathies to all those affected by the earthquakes which struck Kumamoto in April 2016.We have donated 10 million yen through Japanese Red Cross Society to support the rescue and recovery efforts for those affected by the earthquakes.We hope that the affected areas wil l be recovered as soon as possible.We are pleased to report the business results of fiscal year 2015 (62nd business operations) for the period from April 1st, 2015 to March 31st, 2016.
To Our Shareholders
Chairman and CEO
Sachiaki Ibe
Net sales Operating income ( ) / Ordinary income ( ) /Profit attributable to owners of parent ( )
0
20,000
40,000
60,000
80,000
0
2,000
4,000
6,000
8,000
Fiscal Year 2013 Fiscal Year 2014 Fiscal Year 2015
6,790 6,803
5,277
2,6782,770 2,557
4,565 4,450
3,513
61,01261,996 62,475
Fiscal Year 2013 Fiscal Year 2014 Fiscal Year 2015
(Unit: ¥million) (Unit: ¥million)
1
During the fiscal year under review, the Japanese economy is proceeding with moderate recovery based on
background of improvements in the environment for employment and income. However, in the second half
of the fiscal year, factors such as sluggish personal consumption, the slowing down of the economy in
China and in other developing countries and the strengthening of the yen led to increasing in unclear
outlook.
For the pharmaceutical industry, among ethical pharmaceuticals, as a government’s policy of curtailment of
healthcare expenditures, utilizing of generic brand pharmaceuticals is strongly accelerated as compared with
previous years, and competition in OTC drugs market is getting harder. As a consequence, both ethical
pharmaceuticals and OTC drugs remain in such severe situation.
Under such circumstances, on second year of the 8th Mid-Term Management Plan (3 year term starting
from fiscal year 2014 to fiscal year 2016), Zeria proactively continued to invest resources on business. In July
2015 Tillotts Pharma AG, a wholly owned subsidiary of Zeria, acquired from AstraZeneca the global rights to
the manufacture and sale excluding the United States for the inflammatory bowel disease therapeutic
agent, Entocort®. Also, in September 2015 Zeria acquired 49% of the issued shares of the Vietnamese
pharmaceutical manufacturing and sales company, Pharmaceutical Joint Stock Company of February 3rd,
marking the first step forward for the expansion of the business in Asia. As well as steadily reinforcing its
foundation as a global company, Zeria has worked to drive forward the Ethical Pharmaceuticals and the
Consumer Healthcare businesses closely together, which have long been regarded as the inseparable “two
wheels of a cart” of the Group.
As a result of these activities, net sales for the fiscal year under review were 62,475 million yen (up 2.4%
from the previous fiscal year). Operating income was 4,565 million yen (up 70.4%), ordinary income was
4,450 million yen (up 60.7%) and profit attributable to owners of parent was 3,513 million yen (up 37.4%).
In fiscal year 2015, the overseas sales to net sales ratio was 20.0%, compared with 17.2% in the previous
fiscal year.
2
53.9%(Net sales composition ratio)
Asacol
Acinon
Promac
Other
ConsumerHealthcareBusiness
Ethical Pharmaceuticals Business
Net sales
Net sales of major products
Consolidated net sales in Ethical Pharmaceuticals Business
¥33,580 million
Asacol ¥18.25 billion
Promac ¥3.43 billion
Acinon ¥2.96 billion
0
30,000
20,000
25,000
35,000
40,000
Fiscal Year 2013 Fiscal Year 2015
33,58033,759
Fiscal Year 2014
36,430
(Unit: ¥million)
down 0.5%from the previous fiscal year
In the Ethical Pharmaceuticals business, according to basis of compliance with promotion codes, Zeria sought to improve the quality of its medical representatives (MRs), and took steps to upgrade its medical information activities.As for the main product Asacol®, a therapeutic agent for ulcerative colitis, sales grew satisfactorily in Japan. However, overseas sales of the product was hit by the strengthening of the Swiss franc that caused by removal of the ceiling for the Swiss franc versus the Euro by the Swiss National Bank, leading to flat overall. Sales of other products including Acinon®, an H2 receptor antagonist, and Promac®, a zinc-containing antiulcer agent, struggled due to the promotion of generic brand pharmaceuticals. As for Acofide®, the therapeutic agent for functional dyspepsia, although the development of the market is beh ind schedu le , we a re work ing to promote development by raising awareness of both disease and treatment methods in medical institutions.As a result of these, net sales in the business amounted to 33,580 million yen (down 0.5% from the previous fiscal year). Furthermore, Entocort® began contributing to sales and profits for the fiscal year under review from the third quarter, when rights of the product were acquired, and going forward we will build up the product to become a main product for this business.
Summary of Our Business Operations (Consolidated)
3
EthicalPharmaceuticalsBusiness
46.1%(Net sales composition ratio)
Chondroitin range
WithOne range
Other
Hepalyse range
Consumer Healthcare Business
Net sales
Net sales of major products
Consolidated net sales in Consumer Healthcare Business
¥28,741 million
Hepalyse range ¥10.52 billion
Chondroitin range ¥7.41 billion
WithOne range ¥1.60 billion
0
25,000
15,000
20,000
30,000
Fiscal Year 2013 Fiscal Year 2015
27,095
Fiscal Year 2014
25,389
28,741(Unit: ¥million)
In the Consumer Healthcare business, on the progress of the super-aged society, Zeria worked to develop markets through the supply of products which support self-medication for the consumer.As for the main product range, Hepalyse® range, intensive advertising activities such as TV advertisements resulted in sales growth and further enhancement of product awareness. Moreover, in order to strengthen the Hepalyse® W product range which has an aim for selling in convenience stores, we launched Hepalyse® W Sparkling (a carbonated drink) in June 2015 and Hepalyse® W Premium (a soft drink) in March 2016. In addition, to strengthen the OTC drug Hepalyse® series which are nutrients and tonics for physical fatigue and exhaustion, we launched Hepalyse® Plus II in October 2015 . Regard ing Chondro i t in p roduc t r ange , overwhelming market share was maintained firmly as a result of sales activities that promoted its effectiveness, safety and high quality as a range of pharmaceuticals and c lear ly d ist inguished i t f rom health foods. Moreover, as for Chondroitin ZS Tablets®, we launched a product that was smaller and easier to take in October 2015.As a result, net sales in the business amounted to 28,741 million yen (up 6.1% from the previous fiscal year).
OTC drugs
Hepalyse® W series
up 6.1%from the previous fiscal year
4
In the Research and Development division, Zeria is
actively promoting overseas clinical trials of its own
original drugs. At the same time, Zeria acquires in-
licensed drugs that have gained global success and
develops them for the Japanese market.
As part of its efforts to strengthen its new drug pipeline
in the priority gastrointestinal field, Zeria has jointly
conducted a Phase III trial for additional dosages and
administration for Z-206 (Asacol®), with Kyowa Hakko
Kirin Co., Ltd for ulcerative colitis. The trial has been
completed and Zeria is preparing an application for its
approval. Regarding development of Asacol in China,
Zeria also submitted an application for its approval in
May 2013 following the completion of a Phase III trial.
As for Zeria’s own original drug Z-338 (Acofide®), it is
conducting a Phase III trial in patients with functional
dyspepsia in Europe.
Zeria is implementing a Phase II trial for Z-215, a long
lasting proton pump inhibitor and in-licensed drug from
Eisai Co., Ltd., in patients with reflux esophagitis.
In addition, Zeria is conducting a global Phase III clinical
trial for Z-100 which is targeting for cure of cervical
cancer, in the Asian region including Japan.
As for Z-360, Zeria is implementing a global Phase II
clinical trial in the Asian region including Japan in
patients with pancreatic cancer.
Zeria started a Phase III trial for Z-213, a treatment for
iron deficiency anemia and in-licensed drug from Vifor
(International) AG, Switzerland.
Moreover, with regard to development of Entocort® in
Japan, in October 2015 Zeria submitted an application
for its approval for manufacturing and sale under the
brand name Zentacort®.
In the area of Consumer Healthcare products, as well as
pushing ahead with the development of European
herbal medicines Zeria is also launching new products
one after the other.
Meanwhile, Zeria Group company Tillotts Pharma AG is
developing therapeutic drugs for lower gastrointestinal
disease primarily in Europe.
Tillotts Pharma AG is conducting a Phase III trial in
Europe and Canada for an improved mesalazine
formulation benefiting from new technology targeting
ulcerative colitis (Tillotts Pharma development code:
TP05).
In addition, being co-developed with Cancer Prevention
Pharmaceuticals, Inc. (USA), Tillotts Pharma AG is
conducting a Phase III trial in Europe and the USA for
development as a therapeutic agent targeting familial
adenomatous polyposis currently (Tillotts Pharma
development code: TP09).
As a result of these activities, research and development
expenses for the fiscal year under review decreased from
the results of the previous fiscal year to 8,579 million yen
(down 13.2% from the previous fiscal year).
Status of Research and Development
5
I. Domestic
1) Gastrointestinal field
Stage Development Code/Generic Name Development Indications Classification Source
NDA filed Budesonide(Scheduled product name: Zentacort) AstraZeneca Crohn’s disease Glucocorticoid In-licensed
Preparing for filing Z-206/Mesalazine(Asacol® additional dosage and administration)
Zeria (Co-development with Kyowa Hakko Kirin) Ulcerative colitis pH-dependent controlled-release
formulationOriginal(Tillotts Pharma AG)
Phase II(Asia Global Development) Z-360 Zeria Pancreatic cancer Gastrin CCK2 receptor antagonist Original
Phase II Z-215 Zeria Acid-related disorders Long lasting proton pump inhibitor In-licensed
2) Other fields
Stage Development Code/Generic Name Development Indications Classification Source
Phase III(Asia Global Development) Z-100 Zeria Cervical cancer Immunomodulator Original
Phase III Z-213/Ferric carboxymaltose Zeria Iron deficiency anemia Intravenous iron replacement In-licensed
II. Overseas
Stage Development Code/Generic Name Development Indications Classification Source
NDA filed(China) Z-206/Mesalazine Co-development
of Zeria and Tillotts Pharma Ulcerative colitis pH-dependent controlled-releaseformulation
Original (Tillotts Pharma AG)
Phase III(Europe) Z-338/Acotiamide Zeria Functional dyspepsia Upper gastrointestinal motility
modulator Original
Phase III(Asia) Z-100 Zeria Cervical cancer Immunomodulator Original
Phase III(Europe, Canada) TP05/Mesalazine Tillotts Pharma Ulcerative colitis OPTICORE formulation Original
(Tillotts Pharma AG)
Phase III(Europe, USA) TP09/CPP-1X·Sulindac
Tillotts Pharma (Co-development with Cancer Prevention Pharmaceuticals)
Familial adenomatous polyposis Polyamine biosynthesis suppression In-licensed
Phase II completed(North America) Z-338/Acotiamide Zeria Functional dyspepsia Upper gastrointestinal motility
modulator Original
Phase II(Asia) Z-360 Zeria Pancreatic cancer Gastrin CCK2 receptor antagonist Original
(As of June 29, 2016)
● Status of Pipeline of New Drugs
Phase I Clinical Trials Phase II Clinical Trials Phase III Clinical Trials
Reference
* Placebo: A fake drug that does not contain the active ingredient, but which is indistinguishable from the “drug candidate” by outer appearance or taste, etc.
By administering to a large number of patients, the efficacy, safety and method of use of the “drug candidate” are studied as a final stage. During this phase, the “drug candidate” is tested against other drugs on the market or placebo*. In many cases, stringent testing methods called double-blind trials are performed.
After safety has been confirmed by Phase I clinical trials, the efficacy and safety of the “drug candidate,” as well as the appropriate method of use such as dosage and administration method, are tested on a small number of patients against placebo*.
After confirmation of the efficacy and safety by animal studies, “drug candidates” are tested on a small group of healthy subjects. These trials aim for determination of not only safety, but also how long it takes for the body through an absorption of the drug and the degree to which the body excrete the drug.
Research and Development Pipeline
6
● Status of Production and DistributionIn Zeria’s Production and Distribution division, operation is proceeding with a securing of quality which is set as top priority. In departments related to Production, we are focusing to secure more high quality and reduce cost of goods. In departments related to Distribution, meanwhile, Zeria outsourced logistic operations, and improvement in operational efficiency and cost reductions are proceeded.Furthermore, in order to achieve stable supply of Zeria’s products such as OTC drugs which is expected to rise its demand, Zeria has been carrying out renovation work at the Saitama Plant aiming for increase in production capacity. This renovation was completed in March 2016 and sequential operation is being done. Also, in order to achieve stable supply of drink products which is expected to be higher demand in Tsukuba Plant, we have begun renovation work at the Plant.
● Close-up
A refresh for Chondroitin ZS Tablets®
In the more than 50 years
since launch of Chondroitin ZS
Tablets® in 1964, the drug have
been used by many consumers
who suffer f rom jo int and
lumbar pain as an oral drug.
In response to consumers who
commented that the tablets are
large and difficult to swallow, we have studied repeatedly
the issue of making the tablets smaller. While keeping the
content of the active ingredient, chondroitin sulfate sodium
(260mg per tablet, 1,560mg/6 tablets daily dose), we were
able to reduce their size, making them easier to swallow.
At the same time, we changed the sweetener from
saccharin sodium to acesulfame potassium and reduced
the flavoring, giving it an aroma and taste that is easier to
take.
62nd Term 63rd Term (Forecast)
Net Sales¥62,475 million
up 2.4% ( from the previous fiscal year )¥66,000 million
up 5.6% ( from the previous fiscal year )
Operating Income¥4,565 million
up 70.4%( from the previous fiscal year )¥4,800 million
up 5.1% ( from the previous fiscal year )
Ordinary Income¥4,450 million
up 60.7% ( from the previous fiscal year )¥4,600 million
up 3.4% ( from the previous fiscal year )Profit Attributable to Owners of Parent
¥3,513 millionup 37.4% ( from the previous fiscal year )
¥3,600 millionup 2.5% ( from the previous fiscal year )
● Outlook for Fiscal Year 2016Regarding outlook for the consolidated results of fiscal year 2016 (ending March 31, 2017), Zeria forecasts that it will secure increases in both sales and profits, with net sales of 66.0 billion yen (up 5.6% from the previous fiscal year), operating income of 4.8 billion yen (up 5.1%), ordinary income of 4.6 billion yen (up 3.4%), and profit attributable to owners of parent of 3.6 billion yen (up 2.5%).
Net salesIn the Ethical Pharmaceuticals business, Zeria expects an increase in sales resulting from overseas sales growth of Asacol® which is the therapeutic agent for ulcerative colitis, full-year contribution of Entocort® which is a therapeutic agent for inflammatory bowel disease, and buildup of the domestic market for Acofide® which is a therapeutic agent for functional dyspepsia, despite continuing difficult conditions caused by NHI price reductions and impact of generic brands in Japan. In the Consumer Healthcare business, Zeria expects increases in sales from sales growth of the Hepalyse® product range and the Chondroitin product range due to the contribution of new products as the main driver.
IncomeDespite expectations that research and development expenses will continue to be high because of the progress in clinical trials being conducted in and outside Japan, and advertising expenses will be increased, Zeria forecasts higher operating income, ordinary income and profit attributable to owners of parent compared with the fiscal year under review, due to increased sales of main products.
Status of Production and Distribution / Outlook for Fiscal Year 2016
7
Soft drinks, Designated quasi-drug, Food for specified health uses
Set of aluminum can drinks and Hepalyse® W
Cosmetics and health products
Set of ChondroMax® and Aposty®
Health drink
2 bottles of Chondrobe® Concentrate, JUNKOU®
Zeria offers a hospitality program to its shareholders in recognition of their constant support.Shareholders who own 1,000 or more of Zeria’s shares can choose from one of the six options A to F. Shareholders who own 100 or more but less than 1,000 of Zeria’s shares receive option G.Moreover, from the record date at the end of March 2016, we have added option F.Zeria hopes its shareholders will try the gift products for better understanding of its wide-ranging product structure.
A
D
E
F
G
B
C
Option
Option
Option
Option
Option
Option
Option
Chondroitin-Content Intensive Nighttime Essence
2 bottles of ZZ:CC® ADSORB ESSENCE (30g)
* This product may be bought at Zeria’s online store at http://www.zeriaonline.com/.
* This product may be bought at Zeria’s online store at http://www.zeriaonline.com/.
Three-product Quality Moisturizer Set
IONA Three-product Basic Skincare Set
High-purity chondroitin with natural ions to moisturize and give
firmness to aging skin
IONA R Two-product Special Care Set
Drink containing liver extract and turmeric extract
10 bottles of Hepalyse® W
Special Offers to Our Shareholders
8
Tillotts Pharma AG acquires the rights to Entocort®, a therapeutic agent for Crohn’s disease.
On July 8, 2015, Tillotts Pharma AG, a wholly owned subsidiary
of Zeria, acquired from AstraZeneca the global rights to the
manufacture and sale excluding the United States for the Crohn’s
disease therapeutic agent Entocort® (generic name: budesonide).
Entocort® is first-line glucocorticoid therapy, currently approved in
more than 40 countries for the treatment of Crohn’s disease (CD).
Because it acts at inflamed site of the digestive tract, it has the
advantage that side effects are reduced.
Due to acquisition of the rights, in addition to the therapeutic
agent for ulcerative colitis Asacol®, it has become possible for
Tillotts Pharma AG to sell the Crohn’s disease therapeutic agent
Entocort®, significantly increasing its presence in the area of
the digestive system. At the same time, we anticipate that by
expanding the sales area of Entocort® Tillotts Pharma AG can
achieve a strengthening of its business base, primarily in Europe
while making a contribution to the further development of the
Group.
Moreover, in Japan Zeria has submitted application for approval of
Zentacort® and, after its approval we assume that in combination
with Asacol®, the therapeutic agent for ulcerative colitis, we
can make a considerable contribution to the treatment of
inflammatory bowel disease in Japan (both ulcerative colitis and
Crohn’s disease).
Topics
9
Hepalyse® W Premium is newly marketed
Hepalyse® W Premium was launched on March 21, 2016 in convenience stores across Japan as a new product in the
Hepalyse® W soft-drink series, which is aimed at convenience stores.
In its range of Hepalyse® brand products for convenience stores, Zeria has been selling the soft drinks Hepalyse® W and
Hepalyse® W Hyper, the carbonated drink Hepalyse® W Sparkling, the designated quasi-drug drink Hepalyse® Amino
and the dietary supplement Hepalyse® W (Pastille Type) at convenience stores nationwide. These products have garnered
immense praise.
Recently we added Hepalyse® W Premium to the line-up, containing 2.5 times the liver extract compared to Hepalyse® W in
order to support those who are concerned about their health.
Character of Hepalyse® W Premium
■ Premium drink that represents the highest grade in the
Hepalyse® W series.
Contains at highest amount of liver extract (250mg) and
chondroitin (100mg) among all the Hepalyse® W series. It is
a premium version of Hepalyse® W that also contains 45mg
of turmeric extract (curcumin) for those times when it really
matters.
■ A refreshing apple taste
Has been carefully finished to give a refreshing apple taste.
Despite increasing the amount of liver extract, it remains as
easy to drink and as pleasant as it was previously.
■ The other delightful ingredients are unchanged
Includes extract of black pepper to aid the absorption of the turmeric extract (curcumin) and vitamins.
10
Financial Statements (Consolidated)
Consolidated Balance Sheets (Summary)
TermItem
Previous Fiscal Year Current Fiscal Year
(As of March 31, 2015) (As of March 31, 2016)
Assets
Current Assets 45,680 39,695
Cash and Deposits 18,012 12,343
Notes and Accounts Receivable-Trade 16,241 14,763
Inventories 8,189 8,013
Deferred Tax Assets 943 744
Other 2,312 3,869
Allowance for Doubtful Accounts (18) (39)
Noncurrent Assets 50,587 79,482
Property, Plant and Equipment 22,021 23,274
Buildings and Structures 7,092 8,428
Machinery, Equipment and Vehicles 2,008 2,635
Land 11,579 11,671
Construction in Progress 940 143
Other 401 394
Intangible Assets 12,344 35,783
Investments and Other Assets 16,221 20,424
Investment Securities 9,731 12,471
Deferred Tax Assets 85 13
Net Defined Benefit Asset 5,400 7,113
Other 1,049 870
Allowance for Doubtful Accounts (44) (43)
Total Assets 96,268 119,178
TermItem
Previous Fiscal Year Current Fiscal Year
(As of March 31, 2015) (As of March 31, 2016)
Liabilities
Current Liabilities 21,911 48,245
Notes and Accounts Payable-Trade 2,383 2,041
Short-Term Loans Payable 11,572 39,037
Other 7,954 7,166
Noncurrent Liabilities 11,786 6,865
Long-Term Loans Payable 10,636 4,653
Net Defined Benefit Liability 371 643
Asset Retirement Obligations 74 75
Other 705 1,492
Total Liabilities 33,697 55,110
Net Assets
Shareholders’ Equity 55,697 56,454
Capital Stock 6,593 6,593
Capital Surplus 12,716 12,055
Retained Earnings 36,392 37,810
Treasury Stock (3) (4)
Accumulated Other Comprehensive Income 6,872 7,280
Valuation Difference on Available-for-Sale Securities 1,474 879
Foreign Currency Translation Adjustment 3,994 4,212
Remeasurements of Defined Benefit Plans 1,403 2,188
Non-Controlling Interests - 332
Total Net Assets 62,570 64,067
Total Liabilities and Net Assets 96,268 119,178
(Unit: ¥million*)
Unit: ¥million rounded down to nearest million
11
Consolidated Statements of Income (Summary) (Unit: ¥million*) Consolidated Statements of Cash Flows (Summary) (Unit: ¥million*)
TermItem
Previous Fiscal Year Current Fiscal Year
(From April 1, 2014 (From April 1, 2015
to March 31, 2015) to March 31, 2016)
Net Sales 61,012 62,475Cost of Sales 18,521 17,930Gross Profit 42,491 44,544Reversal of Provision for Sales Returns 110 62Provision for Sales Returns 62 58Gross Profit-Net 42,539 44,548Selling, General and Administrative Expenses 39,861 39,982Operating Income 2,678 4,565Non-Operating Income 338 352Non-Operating Expenses 246 467Ordinary Income 2,770 4,450Extraordinary Income 1,507 1,091Extraordinary Loss 457 280Income before Income Taxes 3,819 5,262Income Taxes-Current 1,315 602Income Taxes-Deferred (53) 1,127Net Profit 2,557 3,532Profit Attributable to Non-Controlling Interests - 18Profit Attributable to Owners of Parent 2,557 3,513
TermItem
Previous Fiscal Year Current Fiscal Year
(From April 1, 2014 (From April 1, 2015
to March 31, 2015) to March 31, 2016)
Net Cash Provided by (Used in) Operating Activities 653 5,694
Net Cash Provided by (Used in) Investing Activities 475 (32,709)
Net Cash Provided by (Used in) Financing Activities (5,839) 22,416
Effect of Exchange Rate Change on Cash and Cash Equivalents 177 (1,070)
Net Increase (Decrease) in Cash and Cash Equivalents (4,533) (5,669)
Cash and Cash Equivalents at Beginning of Year 22,070 17,880
Net Increase (Decrease) in Cash and Cash Equivalents Resulting from Change of Scope of Consolidation
343 -
Cash and Cash Equivalents at End of Year 17,880 12,210
Unit: ¥million rounded down to nearest million
Unit: ¥million rounded down to nearest million
Consolidated Statements of Changes in Net Assets (Summary) (From April 1, 2015 to March 31, 2016)(Unit: ¥million*)
Shareholders’ Equity Accumulated Other Comprehensive IncomeNon-
Controlling Interests
Total Net AssetsCapital
StockCapital Surplus
Retained Earnings
Treasury Stock
Total Shareholders’
Equity
Valuation Difference on Available-for-Sale Securities
Foreign Currency
Translation Adjustment
Remeasurements of Defined
Benefit Plans
Total Accumulated Other
Comprehensive Income
Balance at the Beginning of Current Period 6,593 12,716 36,392 (3) 55,697 1,474 3,994 1,403 6,872 - 62,570Cumulative Effects of Changes in Accounting Policies (660) (501) (1,162) (95) (95) (1,258)
Balance at the Beginning of Current Period Reflecting Changes in Accounting Policies 6,593 12,055 35,890 (3) 54,535 1,474 3,898 1,403 6,776 - 61,312
Changes of Items during the Period
Change of Scope of Consolidation - -Dividends from Surplus (1,593) (1,593) (1,593)Profit Attributable to Owners of Parent 3,513 3,513 3,513Purchase of Treasury Stock (0) (0) (0)Net Changes of Items Other than Shareholders’ Equity (595) 314 784 503 332 835
Total Changes of Items during the Period - - 1,920 (0) 1,919 (595) 314 784 503 332 2,755Balance at the End of Current Period 6,593 12,055 37,810 (4) 56,454 879 4,212 2,188 7,280 332 64,067
Unit: ¥million rounded down to nearest million
12
• Tillotts Pharma AG (Switzerland)
• ZPD A/S (Denmark)
• Zeria Healthway Co., Ltd.
• Tillotts Pharma AB (Sweden)
• Tillotts Pharma Ltd. (Ireland)
• Tillotts Pharma UK Ltd. (United Kingdom)
• Tillotts Pharma Czech s.r.o. (Czech Republic)
• Tillotts Pharma Spain S.L.U. (Spain)
• Tillotts Pharma GmbH (Germany)
• IONA INTERNATIONAL CORPORATION
• Zevice Co., Ltd.
• Pharmaceutical Joint Stock Company of February 3rd (Vietnam)
Established: December 1955
Paid-in Capital: ¥6,593,398,500
Number of Employees: 1,799 (Consolidated)
Business Activities: 1. Manufacturing, sales, import and export of pharmaceuticals, quasi-drugs and reagents.
2. Manufacturing, sales, import and export of cosmetics, health foods, soft drinks, hygienic goods and medical devices.
Company Outline Place of Business
Number of Consolidated Subsidiaries: 12
Directors and Audit & Supervisory Board Members (As of June 29, 2016)
• Headquarters • Keiji Sales Office
• Sapporo Branch • Hokuriku Sales Office
• Sendai Branch • Chugoku & Shikoku Branch
• Tokyo Branch • Okayama Sales Office
• Tokyo 3rd Sales Office • Takamatsu Sales Office
• Kanagawa 1st and 2nd Sales Office • Fukuoka Branch
• Saitama Sales Office • Central Research Laboratories
• Chiba Sales Office • Saitama Plant
• Kita Kanto Sales Office • Tsukuba Plant
• Koshinetsu Sales Office • Tokyo Distribution Center
• Nagoya Branch • Sapporo Distribution Center
• Shizuoka Sales Office • Saitama Distribution Center
• Osaka Branch • Osaka Distribution Center
• Osaka 2nd Sales Office • Kyushu Distribution Center
• Kobe Sales Office
• Other Sales OfficeAomori, Utsunomiya, Kanetsu, Takasaki, Yamaguchi, Yonago, Matsuyama, Kochi, Nagasaki, Kumamoto, Oita, Kagoshima, Okinawa
Chairman and CEO Sachiaki Ibe
President and COO Mitsuhiro Ibe
Executive Vice President Hirokazu Endo
Managing Director Makoto Kishimoto
Director Akira Ohno
Director Tetsuo Komori
Director Masahiro Fukahori
Director Hiroki Kato
Director Yoshihiro Hiraga
Director Katsuyuki Ishii
Director Hidekazu Yokote
Director Toshiaki Kawagoe
Director Mitsuyuki Yoshijima
Audit & Supervisory Board Member Koujirou Takami
Audit & Supervisory Board Member Shigeya Furuhata
Audit & Supervisory Board Member (Outside) Yukiko Naka
Audit & Supervisory Board Member (Outside) Hiroshi Wakabayashi
Company Information (As of March 31, 2016)
13
Major Shareholders
Name of Shareholder Number of Shares Held
Percentage Held (%)
Ibe Corporation 4,741,847 8.9
Japan Trustee Service Bank, Ltd. (Trust Account) 2,609,900 4.9
The Bank of Tokyo-Mitsubishi UFJ, Ltd. 2,107,050 4.0
Morinaga Milk Industry Co., Ltd. 2,040,215 3.8
Sachiaki Ibe 1,592,967 3.0
Zeria Pharmaceutical Co., Ltd. Employee Stockholding Plan 1,433,864 2.7
Sumitomo Mitsui Banking Corporation 1,406,131 2.6
Mizuho Bank, Ltd. 1,406,053 2.6
Resona Bank, Limited 1,182,385 2.2
Aioi Nissay Dowa Insurance Co., Ltd. 944,560 1.8
(Note) The percentage held is calculated by subtracting treasury stock (totaling 3,871 shares).
Share Price and Trading Volume
Distribution of Shares by Shareholder Type
(i) Number of authorized shares: 119,860,000 shares
(ii) Number of shares outstanding: 53,119,190 shares
(iii) Number of shareholders: 16,919
Status of Shares
Financial Institutions17,469,006 shares (32.89%)
Other DomesticCorporations17,704,996 shares(33.33%)
Foreigners2,833,557 shares(5.34%)
Financial Instruments Business331,644 shares(0.62%)
Individual Shareholdersand Others14,779,987 shares(27.82%)
Distribution Ratio of Shares
Total53,119,190 shares
1,000
2,000
3,000
4,000
5,000
500
1,000
1,500
2,500
2,000
0 02016
JanuaryOctober November December February MarchJuly2015April May June August September
Share Price (¥)
Number of Shares Traded (1,000 shares)
Share Information (As of March 31, 2016)
14
Please refer to latest IR information on our website.The Company has set up a website for the purpose of providing accurate
information on a timely basis. The website contains a broad array of information
useful for shareholders and investors, from IR information to the latest news.
http://www.zeria.co.jp/english/
10-11 Nihonbashi-kobunacho, Chuo-ku, Tokyo 103-8351TEL 03-3663-2351 (Main) FAX 03-3663-2352
03-3661-2080http://www.zeria.co.jp/
Customer Service, Zeria Pharmaceutical Co., Ltd.
Shareholder Memo
Fiscal Year
Ordinary General Meeting of Shareholders
Record Date
Transfer Agent
Account Management Institution for Special Account
Mailing Address (Inquiry information)
From April 1st of each year to March 31st of the following year
Late June of each year
Ordinary General Meeting of Shareholders and end of term dividend: March 31 of each year Interim dividend: September 30 of each year
Sumitomo Mitsui Trust Bank, Limited 1-4-1 Marunouchi, Chiyoda-ku, Tokyo
Sumitomo Mitsui Trust Bank, Limited 1-4-1 Marunouchi, Chiyoda-ku, Tokyo
Stock Transfer Agency Business Planning Department, Sumitomo Mitsui Trust Bank, Limited 2-8-4 Izumi, Suginami-ku, Tokyo 168-0063 TEL: 0120-782-031 (toll-free) Handling operation is conducted in main branch and all domestic branches of Sumitomo Mitsui Trust Bank, Limited.
● Applications for change of address or for purchase demands of
fractional shares, etc.
Please send such notifications or applications to the securities company
where your account is held.
For shareholders for whom a special account has been opened because
there is no account held by a securities company, please send such
notifications or applications to Sumitomo Mitsui Trust Bank, Limited, the
account management institution for the special account.
● Applications for payment of dividends payable
Please send such applications to the transfer agent, Sumitomo Mitsui
Trust Bank, Limited.
● Statement of Dividend Calculation
The “Statement of Dividend Calculation” that is sent to shareholders at
the time of dividends payment serves as your “Payment Notification
Statement,” based on the provisions of the Act on Special Measures
Concerning Taxation. When you file your final tax return, you can use this
document as the accompanying documentation.
Shareholders who receive payment of dividends by the dividend warrant
shall also receive the “Statement of Dividend Calculation.” Shareholders
who file final tax returns should store this document in a secure place.